Synthesis of amino acids and related compounds. 29. Synthesis and hypolipidemic activities of 5-thienyl-4-oxazoleacetic acid derivatives
作者:Tamon Moriya、Seiichi Takabe、Sadao Maeda、Kazuo Matsumoto
DOI:10.1021/jm00153a006
日期:1986.3
A series of 2,5-disubstituted 4-oxazoleacetic acid derivatives was synthesized and evaluated for hypolipidemic activity. Among them, those with a thienyl group at C-5 of the oxazole ring exerted highly potent hypolipidemic effects in rats. 2-(4-Fluorophenyl)-5-(3-thienyl)-4-oxazoleacetic acid (88) was the most potent derivative: it was about 2 times as active in normal SD male rats and about 4 times
合成了一系列2,5-二取代的4-恶唑乙酸衍生物,并评估了其降血脂活性。其中,在恶唑环的C-5处具有噻吩基的化合物在大鼠中具有强效的降血脂作用。2-(4-氟苯基)-5-(3-噻吩基)-4-恶唑乙酸(88)是最有效的衍生物:它在正常SD雄性大鼠中的活性约为2倍,而在遗传性高脂血症中的活性约为4倍。大鼠(THLR / 1)为氯氟贝特,抗动脉硬化指数得到改善(HDL-Cho / Total-Cho)。另外,它显示出离体血小板聚集的抑制。